Biological significance and pathophysiological role of Matrix Metalloproteinases in the Central Nervous System

被引:6
作者
Ganguly, Krishnendu [1 ]
Adhikary, Krishnendu [1 ]
Acharjee, Arup [2 ]
Acharjee, Papia [3 ]
Trigun, Surendra Kumar [3 ]
Mutlaq, Alaa Saeed [4 ]
Ashique, Sumel [5 ,6 ]
Yasmin, Sabina [7 ]
Alshahrani, Asma M. [8 ,9 ]
Ansari, Mohammad Yousuf [10 ]
机构
[1] Paramed Coll Durgapur, Dept Med, Lab Technol, Durgapur 713212, W Bengal, India
[2] Univ Allahabad, Dept Zool, Mol Om Lab, Allahabad, Uttar Pradesh, India
[3] Banaras Hindu Univ, Dept Zool, Biochem Sect, Varanasi 221005, Uttar Pradesh, India
[4] Saudi Minist Hlth, Deputy Therapeut, Riyadh, Saudi Arabia
[5] Lovely Profess Univ, Sch Pharmaceut Sci, Phagwara 144411, Punjab, India
[6] Bengal Coll Pharmaceut Sci & Res, Dept Pharmaceut, Durgapur 713212, W Bengal, India
[7] King Khalid Univ, Coll Pharm, Dept Pharmaceut Chem, Abha 62529, Saudi Arabia
[8] King Khalid Univ, Fac Pharm, Dept Clin Pharm, Abha, Saudi Arabia
[9] Shaqra Univ, Dept Clin Pharm, Shaqraa, Saudi Arabia
[10] Maharishi Markandeshwar Deemed Univ, MM Coll Pharm, Ambala 133207, Haryana, India
关键词
Matrix Metalloproteinase; Extracellular matrix; Synaptic Plasticity; Stress; Depression; Addiction; BLOOD-BRAIN-BARRIER; LONG-TERM POTENTIATION; FRAGILE-X-SYNDROME; GENE KNOCK-OUT; FACTOR METABOLIC DYSFUNCTION; MESSENGER-RNA EXPRESSION; FOCAL CEREBRAL-ISCHEMIA; SPINAL-CORD INJURY; GELATINASE B MMP-9; TISSUE INHIBITOR;
D O I
10.1016/j.ijbiomac.2024.135967
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Matrix Metalloproteinases (MMPs), which are endopeptidase reliant on zinc, are low in embryonic tissues but increases in response to a variety of physiological stimulus and pathological stresses. Neuro-glial cells, endothelial cells, fibroblasts, and leucocytes secrete MMPs, which cleave extracellular matrix proteins in a time- dependent manner. MMPs affect synaptic plasticity and the development of short-term memory by controlling the size, shape, and excitatory synapses' function through the lateral diffusion of receptors. In addition, MMPs influence the Extracellular Matrix proteins in the Peri-Neuronal Net at the Neuro-glial interface, which aids in the establishment of long-term memory. Through modulating neuronal, and glial cells migration, differentiation, Neurogenesis, and survival, MMPs impact brain development in mammals. In adult brains, MMPs play a beneficial role in physiological plasticity, which includes learning, memory consolidation, social interaction, and complex behaviors, by proteolytically altering a wide variety of factors, including growth factors, cytokines, receptors, DNA repair enzymes, and matrix proteins. Additionally, stress, depression, addiction, hepatic encephalopathy, and stroke may all have negative effects on MMPs. In addition to their role in glioblastoma development, MMPs influence neurological diseases such as epilepsy, schizophrenia, autism spectrum disorder, brain damage, pain, neurodegeneration, and Alzheimer's and Parkinson's. To help shed light on the potential of MMPs as a therapeutic target for neurodegenerative diseases, this review summarizes their regulation, mode of action, and participation in brain physiological plasticity and pathological damage. Finally, by employing different MMP-based nanotools and inhibitors, MMPs may also be utilized to map the anatomical and functional connectome of the brain, analyze its secretome, and treat neurodegenerative illnesses.
引用
收藏
页数:24
相关论文
共 373 条
[1]  
Abdallah Morsi W, 2013, J Mol Psychiatry, V1, P16, DOI 10.1186/2049-9256-1-16
[2]   Amniotic Fluid MMP-9 and Neurotrophins in Autism Spectrum Disorders: An Exploratory Study [J].
Abdallah, Morsi W. ;
Pearce, Brad D. ;
Larsen, Nanna ;
Greaves-Lord, Kirstin ;
Norgaard-Pedersen, Bent ;
Hougaard, David M. ;
Mortensen, Erik L. ;
Grove, Jakob .
AUTISM RESEARCH, 2012, 5 (06) :428-433
[3]   Gelatinases (MMP-2 and MMP-9) are preferentially expressed by Th1 vs. Th2 cells [J].
Abraham, M ;
Shapiro, S ;
Karni, A ;
Weiner, HL ;
Miller, A .
JOURNAL OF NEUROIMMUNOLOGY, 2005, 163 (1-2) :157-164
[4]   Dystroglycan is selectively cleaved at the parenchymal basement membrane at sites of leukocyte extravasation in experimental autoimmune encephalomyelitis [J].
Agrawal, S ;
Anderson, P ;
Durbeej, M ;
van Rooijen, N ;
Ivars, F ;
Opdenakker, G ;
Sorokin, LM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2006, 203 (04) :1007-1019
[5]   MMPs in the central nervous system: Where the good guys go bad [J].
Agrawal, Smriti M. ;
Lau, Lorraine ;
Yong, V. Wee .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2008, 19 (01) :42-51
[6]   REGULATION AND FUNCTION OF ADULT NEUROGENESIS: FROM GENES TO COGNITION [J].
Aimone, James B. ;
Li, Yan ;
Lee, Star W. ;
Clemenson, Gregory D. ;
Deng, Wei ;
Gage, Fred H. .
PHYSIOLOGICAL REVIEWS, 2014, 94 (04) :991-1026
[7]   The neurobiology of social environmental risk for schizophrenia: an evolving research field [J].
Akdeniz, Ceren ;
Tost, Heike ;
Meyer-Lindenberg, Andreas .
SOCIAL PSYCHIATRY AND PSYCHIATRIC EPIDEMIOLOGY, 2014, 49 (04) :507-517
[8]   Differences in metalloproteinases and their tissue inhibitors in the cerebrospinal fluid are associated with delirium [J].
Aksnes, Mari ;
Schibstad, Mari Haavig ;
Chaudhry, Farrukh Abbas ;
Neerland, Bjorn Erik ;
Caplan, Gideon ;
Saltvedt, Ingvild ;
Eldholm, Rannveig S. ;
Myrstad, Marius ;
Edwin, Trine Holt ;
Persson, Karin ;
Idland, Ane-Victoria ;
Pollmann, Christian Thomas ;
Olsen, Roy Bjorkholt ;
Wyller, Torgeir Bruun ;
Zetterberg, Henrik ;
Cunningham, Emma ;
Watne, Leiv Otto .
COMMUNICATIONS MEDICINE, 2024, 4 (01)
[9]   Alterations in serum MMP-8, MMP-9, IL-12p40 and IL-23 in multiple sclerosis patients treated with interferon-β1b [J].
Alexander, J. S. ;
Harris, M. K. ;
Wells, S. R. ;
Mills, G. ;
Chalamidas, K. ;
Ganta, V. C. ;
McGee, J. ;
Jennings, M. H. ;
Gonzalez-Toledo, E. ;
Minagar, A. .
MULTIPLE SCLEROSIS JOURNAL, 2010, 16 (07) :801-809
[10]   Adult Hippocampal Neurogenesis in Natural Populations of Mammals [J].
Amrein, Irmgard .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2015, 7 (05) :1-20